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                    Arizona Paid Clinical Trials
A listing of 1697  clinical trials  in Arizona  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            1201 - 1212 of 1697
        
                Arizona is currently home to 1697 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Phoenix, Tucson, Scottsdale and Mesa. Whether you're a healthy volunteer interested in paid medical research or someone seeking trials related to a specific condition, the state offers a diverse array of opportunities in your vicinity.
            
                                                Featured Trial
                
                Healthy Participants Needed (Colonoscopy + Cancer Screening)
            
        Recruiting
            
        Earn $325 - $475 in electronic payment card compensation for your time and effort by participating in a clinical study to develop a blood test that may one day help screen for colon cancer. Take a quick quiz to see if you qualify.
    
    
                            Conditions: 
                                    
        
            
                        Healthy
                    
                                    
                        Healthy Volunteers
                    
                                    
                        Healthy Subjects
                    
                                    
                        Healthy Volunteer
                    
                                    
                        Healthy Participants
                    
                                    Featured Offer
                
                Lose Weight with GLP-1 Medications
            
        Recruiting
            
        Policy Lab has partnered with OnlineSemaglutide.org to offer trusted access to semaglutide and other GLP-1 medications, including generic alternatives to Ozempic® and Wegovy®. 
GLP-1 medications are scientifically backed to help individuals achieve significant weight loss—on average, 15-20% of body weight within a year.
As a valued user, you’re eligible for $50 off your first program with code policy-lab-50.
    GLP-1 medications are scientifically backed to help individuals achieve significant weight loss—on average, 15-20% of body weight within a year.
As a valued user, you’re eligible for $50 off your first program with code policy-lab-50.
                            Conditions: 
                                    
        
            
                        Overweight
                    
                                    
                        Overweight and Obesity
                    
                                    
                        Obesity
                    
                                    
                        Weight Loss
                    
                                    
                        Morbid Obesity
                    
                                    Featured Trial
                
                Stroke Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Stroke
    
    
                            Conditions: 
                                    
        
            
                        Stroke
                    
                                    Featured Trial
                
                Chronic Kidney Disease (CKD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Chronic Kidney Disease (CKD)
    
    
                            Conditions: 
                                    
        
            
                        Chronic Kidney Disease (CKD)
                    
                                    Featured Trial
                
                Ischemic heart disease (IHD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Ischemic heart disease (IHD)
    
    
                            Conditions: 
                                    
        
            
                        Ischemic heart disease (IHD)
                    
                                    
                
                                    Long-Term Safety of Lutetium (177Lu) Vipivotide Tetraxetan in Participants With Prostate Cancer
                                
            
            
        Recruiting
                            
            
                The purpose of this post-marketing study is to further characterize the long-term outcome of known or potential risks of lutetium (177Lu) vipivotide tetraxetan also known as \[177Lu\]Lu-PSMA-617 or 177Lu-PSMA-617 and hereinafter referred to as AAA617. The study also seeks to further characterize (as possible) any other AAA617 causally related serious adverse event(s) in the long-term in adults with prostate cancer who received at least one dose of AAA617 from interventional, Phase I-IV Novartis...  Read More             
        
        
    Gender:
                MALE
            Ages:
                Between 18 years and 100 years
            Trial Updated:
                04/21/2025
            
            Locations: Mayo Clinic Arizona, Scottsdale, Arizona         
        
        
            Conditions: Prostate Cancer
        
            
        
    
                
                                    DALY II USA/ MB-CART2019.1 for DLBCL
                                
            
            
        Recruiting
                            
            
                DALY II USA is a phase II, multi-center, single arm study to evaluate the efficacy, safety, and pharmacokinetics of zamtocabtagene autoleucel (MB-CART2019.1) in patients with relapsed and/or refractory diffuse large B cell lymphoma (DLBCL) after receiving at least two lines of therapy. Additional cohorts include subjects with B-cell primary or secondary central nervous system (CNS) lymphoma (PCNSL) and (SCNSL), mantle cell lymphoma (MCL) and Richter's transformation (RT) after receiving at least...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                04/21/2025
            
            Locations: Banner MD Anderson Cancer Center, Gilbert, Arizona         
        
        
            Conditions: Refractory Diffuse Large B Cell Lymphoma (DLBCL), Relapsed Diffuse Large B Cell Lymphoma, High Grade B-cell Lymphoma (HGBCL), Primary Mediastinal B-cell Lymphoma (PMBCL), Transformed Lymphoma, Central Nervous System Lymphoma, Mantle Cell Lymphoma (MCL), Richter Transformation
        
            
        
    
                
                                    SBRT +/- Pembrolizumab in Patients With Local-Regionally Recurrent or Second Primary Head and Neck Carcinoma
                                
            
            
        Recruiting
                            
            
                This phase II trial with a safety run-in component will evaluate whether the addition of pembrolizumab to Stereotactic Body Radiation Therapy (SBRT) re-irradiation will improve the progression-free survival for patients with recurrent or new second primary Head and Neck Squamous Cell Carcinoma (HNSCC).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                04/21/2025
            
            Locations: University of Arizona Cancer Center - North Campus, Tucson, Arizona         
        
        
            Conditions: Head and Neck Squamous Cell Carcinoma (HNSCC)
        
            
        
    
                
                                    Study of the Safety and Neuroprotective Capacity of Scp776 in Acute Ischemic Stroke
                                
            
            
        Recruiting
                            
            
                A Randomized, Placebo-Controlled, Double-Blind, Multicenter Study of the Safety and Neuroprotective Capacity of Scp776 in Subjects Undergoing Endovascular Thrombectomy for Acute Ischemic Stroke             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                04/19/2025
            
            Locations: HonorHealth Scottsdale Osborn Medical Center, Scottsdale, Arizona         
        
        
            Conditions: Acute Ischemic Stroke (AIS)
        
            
        
    
                
                                    Impact of Bromocriptine on Clinical Outcomes for Peripartum Cardiomyopathy
                                
            
            
        Recruiting
                            
            
                The study will enroll 200 women newly diagnosed with peripartum cardiomyopathy within 5 months postpartum in a randomized placebo controlled trial of bromocriptine therapy to evaluate its impact on myocardial recovery and clinical outcomes. Given that bromocriptine prevents breastfeeding, an additional 50 women with peripartum cardiomyopathy excluded from the trial due to a desire to continue breastfeeding but meeting all other entry criteria will be followed in an observational cohort.             
        
        
    Gender:
                FEMALE
            Ages:
                18 years and above
            Trial Updated:
                04/19/2025
            
            Locations: University of Arizona Sarver Heart Center, Tucson, Arizona         
        
        
            Conditions: Peripartum Cardiomyopathy, Postpartum
        
            
        
    
                
                                    Understanding the Mechanisms of Clonal and Non-clonal Cytopenia Following CAR-T Therapy for Multiple Myeloma or CD19+ Lymphoproliferative Disorder (LPD)
                                
            
            
        Recruiting
                            
            
                This clinical trial evaluates the impact of preexisting and therapy-emergent germline and somatic variants on cytopenia in patients with multiple myeloma or CD19 positive lymphoproliferative disorder (LPD) following chimeric antigen receptor T-cell (CAR-T) therapy. The most common adverse event after CAR-T therapy is lower than normal blood cells (cytopenia) and up to one third of patients experience cytopenia that last longer than 30 days post-infusion. Germline and somatic variants are changes...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                04/18/2025
            
            Locations: Mayo Clinic in Arizona, Scottsdale, Arizona         
        
        
            Conditions: Lymphoproliferative Disorder, Multiple Myeloma
        
            
        
    
                
                                    NXP800 for the Treatment of Patients With Advanced or Metastatic Cholangiocarcinoma
                                
            
            
        Recruiting
                            
            
                This phase I trial tests the safety, best dose, and effectiveness of NXP800 in treating patients with cholangiocarcinoma that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). NXP800 inhibits a pathway called the heat shock factor 1 (HSF1) pathway. The inhibition of this pathway inhibits proliferation, migration, survival, and me...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                04/18/2025
            
            Locations: Mayo Clinic in Arizona, Scottsdale, Arizona         
        
        
            Conditions: Advanced Cholangiocarcinoma, Metastatic Cholangiocarcinoma, Refractory Cholangiocarcinoma, Stage III Hilar Cholangiocarcinoma AJCC v8, Stage III Intrahepatic Cholangiocarcinoma AJCC v8, Stage IV Hilar Cholangiocarcinoma AJCC v8, Stage IV Intrahepatic Cholangiocarcinoma AJCC v8
        
            
        
    
                
                                    A SMART Trial of Adaptive Exercises to Optimize Aerobic-Fitness Responses
                                
            
            
        Recruiting
                            
            
                The goal of this clinical trial is to test 6 months of aerobic exercise in older adults who are 65 years or older and have mild cognitive impairment (MCI) or probable/possible mild Alzheimer's Disease. The main questions it aims to answer are:
* test the effects of aerobic exercise on aerobic fitness, white matter hyperintensity (WMH) volume, and patient-centered outcomes;
* identify the best exercise to improve aerobic fitness and reduce non-responses over 6 months; and
* examines the mechanis...  Read More             
        
        
    Gender:
                ALL
            Ages:
                65 years and above
            Trial Updated:
                04/18/2025
            
            Locations: Arizona State University, Phoenix, Arizona         
        
        
            Conditions: Mild Cognitive Impairment, Alzheimer Disease, Cognitive Impairment, Cognitive Decline, Memory Loss, Memory Impairment
        
            
        
    
                
                                    A Phase 1/2a Study of IMM-1-104 in Participants With Advanced or Metastatic Solid Tumors
                                
            
            
        Recruiting
                            
            
                This is an open-label, dose-exploration and expansion study to determine the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of IMM-1-104 when administered as monotherapy or in combination with approved agents in participants with RAS-mutated or RAS/MAPK activated advanced or metastatic solid tumors. The dose exploration will identify the candidate recommended Phase 2 candidate optimal dose of IMM-1-104 to further explore the anti-tumor activity of I...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                04/17/2025
            
            Locations: Mayo Clinic, Scottsdale, Arizona         
        
        
            Conditions: Pancreatic Adenocarcinoma, Malignant Melanoma (Cutaneous), Non-small Cell Lung Cancer (NSCLC), Advanced Solid Tumor
        
            
        
    
                
                                    DSLT Performance in Treatment-naïve Patients With Newly Diagnosed Open Angle Glaucoma
                                
            
            
        Recruiting
                            
            
                DSLT demonstrates a ≥ 20% reduction of IOP from pre-treatment baseline in POAG patients naïve of previous glaucoma treatment at 12 months.             
        
        
    Gender:
                ALL
            Ages:
                30 years and above
            Trial Updated:
                04/16/2025
            
            Locations: Barnet Dulaney Perkins Eye Centers, Mesa, Arizona         
        
        
            Conditions: Open Angle Glaucoma (OAG)
        
            
        
    
                
                                    Study of Oral Deucrictibant Soft Capsule for On-Demand Treatment of Angioedema Attacks in Adolescents and Adults With Hereditary Angioedema
                                
            
            
        Recruiting
                            
            
                This is a Phase 3, multicenter, randomized, double-blind, placebo-controlled, 2-period, 2-treatment cross-over study to evaluate the efficacy and safety of orally administered deucrictibant compared to placebo for the on-demand treatment of HAE attacks, including non-severe laryngeal attacks, in participants ≥12 to ≤75 years of age with HAE type 1, type 2, or type 3, a proportion of whom are using long-term prophylactic medication for HAE.             
        
        
    Gender:
                ALL
            Ages:
                Between 12 years and 75 years
            Trial Updated:
                04/16/2025
            
            Locations: Study Site, Paradise Valley, Arizona         
        
        
            Conditions: Hereditary Angioedema, Hereditary Angioedema Type I, Hereditary Angioedema Type II, Hereditary Angioedema Types I and II, Hereditary Angioedema Attack, Hereditary Angioedema With C1 Esterase Inhibitor Deficiency, Hereditary Angioedema - Type 1, Hereditary Angioedema - Type 2, C1 Esterase Inhibitor [C1-INH] Deficiency, C1 Esterase Inhibitor Deficiency, C1 Esterase Inhibitor, Deficiency of, C1 Inhibitor Deficiency, Hereditary Angioedema - Type 3, Hereditary Angioedema Type III
        
            
        
    
                
                                    AAA-SHAPE Pivotal Trial: Abdominal Aortic Aneurysm Sac Healing and Prevention of Expansion
                                
            
            
        Recruiting
                            
            
                To determine the safety and effectiveness of IMPEDE-FX RapidFill to increase the percentage of subjects with shrinkage of the abdominal aortic aneurysm sac when used as an adjunct to on-label endovascular aneurysm repair (EVAR) stent graft treatment in trial subjects considered candidates for elective EVAR.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                04/16/2025
            
            Locations: Honor Health, Scottsdale, Arizona         
        
        
            Conditions: Aortic Aneurysm, Abdominal
        
            
        
    